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Fermentative Production of Naringinase from Aspergillus niger van Tieghem MTCC 2425 Using Citrus Wastes: Process
Vasudha Borkar1, Snehasis Chakraborty1, Jyoti S Gokhale2
1Department of Food Engineering and Technology, Institute of Chemical Technology, Mumbai, 400 019, India.
Applied Biochemistry and Biotechnology
|July 26, 2020
Summary
This study optimized naringinase production from Aspergillus niger using submerged fermentation. The findings provide optimal conditions for enhanced enzyme activity, crucial for debittering citrus juices.
Area of Science:
- Biotechnology
- Enzymology
- Industrial Microbiology
Background:
- Naringinase is essential for debittering citrus juices through enzymatic hydrolysis of naringin.
- Optimizing naringinase production is key for efficient industrial application.
Purpose of the Study:
- To optimize submerged fermentation conditions for enhanced naringinase production by Aspergillus niger MTCC 2425.
- To characterize the partially purified naringinase and assess its stability.
Main Methods:
- Plackett-Burman and Central Composite Designs were used to optimize fermentation parameters (pH, temperature, inducer concentration).
- Naringin from citrus waste served as the inducer.
- Ion exchange chromatography and SDS-PAGE were employed for partial purification and molecular weight determination.
Main Results:
- Optimal fermentation conditions were determined as pH 4.7, 29.8°C, and 14.9 g·L⁻¹ inducer concentration, yielding 545.2 IU·g⁻¹ naringinase activity.
- Partial purification via ion exchange chromatography resulted in a 9.92-fold increase in specific activity (5460 IU·g⁻¹).
- The enzyme exhibited optimal stability at pH 5 and 50°C, retaining full activity for 150 days at 4°C.
Conclusions:
- The optimized submerged fermentation process significantly enhances naringinase production.
- The characterized naringinase demonstrates promising stability for industrial applications in citrus juice debittering.
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